Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Joep van de Vondervoort"'
Autor:
Bobby P. C. Koeleman, Martijn Koetsier, Kees P.J. Braun, Wout J. Weuring, Ivana Dilevska, Jos Hoekman, Ruben van 't Slot, Joep van de Vondervoort
Publikováno v:
The CRISPR Journal. 4:575-582
Dravet syndrome (DS) is a monogenic epileptic encephalopathy caused by loss-of-function mutations in the voltage-gated sodium channel (VGSC) gene SCN1A. DS has an age of onset within the first year of life and severe disease prognosis. In the past ye
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::206a866d06475cd9d2032d3e4c0fc113
https://doi.org/10.1089/crispr.2021.0013
https://doi.org/10.1089/crispr.2021.0013
Autor:
Wout J, Weuring, Ivana, Dilevska, Jos, Hoekman, Joep, van de Vondervoort, Martijn, Koetsier, Ruben H, van 't Slot, Kees P J, Braun, Bobby P C, Koeleman
Publikováno v:
The CRISPR journal. 4(4)
Dravet syndrome (DS) is a monogenic epileptic encephalopathy caused by loss-of-function mutations in the voltage-gated sodium channel (VGSC) gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e26336741dfb211392fb63754f1e47aa
https://pubmed.ncbi.nlm.nih.gov/34406040
https://pubmed.ncbi.nlm.nih.gov/34406040